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[质粒R57与pB322及RP1相互作用过程中形成的共整合体的结构不稳定性。IS1元件在共整合体降解中的可能作用]

[Structural instability of co-integrates formed during interaction of plasmid R57 with pB322 and RP1. Possible role of IS1 element in the degradation of co-integrates].

作者信息

Danilevich V N, Kostiuchenko D A

出版信息

Mol Biol (Mosk). 1986 May-Jun;20(3):683-96.

PMID:3014314
Abstract

The conjugative plasmid R57 determines resistance to ampicillin and chloramphenicol. Earlier it was shown that R57 encodes site-specific recA-independent recombinase, which acts in cis and resolves IS1-mediated cointegrates arising in the Escherichia coli recA cells between R57 and pBR322. In the present work the properties of the cointegrates between R57 and pBR322 or RP1 arising in the E. coli rec+ strains were studied. It was found that the cointegrates between R57 and pBR322, obtained by mating of the respective biplasmid donors of E. coli rec+ and the rec+ recipients, lost as a result of deletion a large DNA segment of R57 containing determinant Cmr. The resulting hybrid replicons preserved determinants Apr and Tcr of pBR322 and the R57 conjugative properties and were structurally identical. By using plasmid RP1ts12, which is temperature-sensitive in replication, it was demonstrated that in cells rec+ the cointegrates between R57 and RP1 are extremely unstable. On storage they undergo structural degradation mainly affecting the RP1 replicon. The degradation products of the hydrid complex had lost their RP1 genes but preserved the R57 functional determinants. For elucidation of the observed phenomena the properties of the IS1-mediated cointegrates between pBR322:Tn9 and plasmid pBR3.1--deletion derivative of RP1 were studied. It was found that insertion of IS1 sometimes resulted in formation of unstable cointegrates capable of resolving and loosing determinant Cmr with a high frequency. It was suggested that IS1 encodes the site-specific recombinase responsible for resolution of the IS1-mediated cointegrates and deletion generation. Expression of this recombinase appears to be dependent on structure of the insertion sites. The possible role of IS1 and recombinase encoded by it in resolution and structural instability of the cointegrates between R57 and pBR322 or RP1 is discussed.

摘要

接合质粒R57决定对氨苄青霉素和氯霉素的抗性。早期研究表明,R57编码位点特异性的不依赖recA的重组酶,该重组酶顺式作用并可解析在大肠杆菌recA细胞中R57与pBR322之间由IS1介导产生的共整合体。在本研究中,对在大肠杆菌rec+菌株中产生的R57与pBR322或RP1之间的共整合体的特性进行了研究。结果发现,通过将大肠杆菌rec+的相应双质粒供体与rec+受体进行接合而获得的R57与pBR322之间的共整合体,由于缺失而丢失了R57中包含Cmr决定簇的一大段DNA片段。所得的杂种复制子保留了pBR322的Apr和Tcr决定簇以及R57的接合特性,并且在结构上是相同的。通过使用在复制中对温度敏感的质粒RP1ts12,证明在rec+细胞中R57与RP1之间的共整合体极其不稳定。在保存过程中,它们会发生结构降解,主要影响RP1复制子。杂种复合体的降解产物失去了其RP1基因,但保留了R57的功能决定簇。为了阐明所观察到的现象,研究了pBR322:Tn9与质粒pBR3.1(RP1的缺失衍生物)之间由IS1介导的共整合体的特性。结果发现,IS1的插入有时会导致形成不稳定的共整合体,这些共整合体能够高频解析并丢失Cmr决定簇。有人提出,IS1编码负责解析IS1介导的共整合体和产生缺失的位点特异性重组酶。该重组酶的表达似乎取决于插入位点的结构。讨论了IS1及其编码的重组酶在R57与pBR322或RP1之间的共整合体的解析和结构不稳定性中的可能作用。

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